תיאור המשרה
Description
Alma, a Sisram Medical company, is a global leader in medical-aesthetic technologies, with over 25 years of experience in energy-based devices (EBD). Over the years, Alma has evolved into an integrated aesthetic and wellness ecosystem that combines medical devices, injectables, diagnostics, and personalized skincare. The company operates in a dynamic, innovation-driven environment, merging advanced technology with deep clinical understanding to create holistic solutions for aesthetic clinics. Alma’s headquarters are in Caesarea, Israel, with business operations in more than 100 countries worldwide.
Establish, build, and lead the V&V team from the ground up, including defining methodologies, processes, and best practices
Manage and mentor a small and growing team of V&V engineers
Lead end to end, comprehensive verification and validation activities for multidisciplinary medical devices, combining technologies such as laser, RF, ultrasound, and physics-based systems
Define, author, and execute rigorous test strategies, validation plans, and protocols for complex systems
Ensure full compliance with medical device regulatory standards, including documentation, traceability, and validation processes
Partner closely with matrixed cross-functional teams including Mechanics, Hardware, Software, System Engineering, Regulatory, Clinical and Quality
Drive continuous improvement of test methodologies, modern tools, and automation capabilities
Support end-to-end product lifecycle activities including design verification, system validation, and post-market activities.
Partner with Operations and NPI (New Product Introduction) groups to ensure seamless transfer from design verification to manufacturing line validation
Manage relationships and scheduling with External Certified Test Houses for safety, EMC, and environmental compliance testing
Requirements
B.Sc. in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Physics, or a related exact science discipline – Mandatory
At least 5 years of hands-on experience leading V&V / QA, testing complex multidisciplinary systems – mandatory
Proven experience working in medical device companies – mandatory
Direct experience with systems integrating multiple technologies (e.g., laser, RF, ultrasound, or similar physical technologies)
Previous experience as a lead / senior role or strong potential for leadership – must
Prior experience in building or scaling testing activities / teams – strong advantage
Strong understanding of V&V processes within regulated environments (FDA, CE, ISO13485, etc.) - mandatory
Deep familiarity with medical device safety and software standards, specifically IEC 60601 (Medical electrical equipment safety) and IEC 62304 (Medical device software lifecycle) – Highly Preferred
Hands-on experience implementing or working with Application Lifecycle Management (ALM) platforms, defect tracking tools (e.g., Jira), and test automation frameworks or data analysis tools (e.g., MATLAB, Python) – Strong Advantag
Strong leadership capabilities with the ability to build a team and drive it forward
Deep, fundamental understanding of system-level methodologies for complex, multi-tiered / multidisciplinary products
Hands-on, proactive, agile approach with the ability to operate in a rapidly growing, evolving development environment
Strong cross-functional communication and stakeholder management skills to bridge design, quality and regulatory groups
High level of personal ownership, structure organizational skills, and uncompromising attention to detail
Ability to balance strategic thinking with hands-on execution
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